FDA Registration
Active
🇺🇸 United States
LifeNet Health Northwest
Reg #: 3009672666
·
FEI: 3009672666
·
Expires 2026
Products
5
Proprietary Names
11
Establishment Types
2
Classifications
5
Registration Details
- Registration Name
- LifeNet Health Northwest
- Registration Number
- 3009672666
- FEI Number
- 3009672666
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- 501 Sw 39th St
- City
- Renton
- State
- WA
- ZIP
- 98057
- Country
- US
Regulatory Submissions
- 510(k) Number
- K053098
Owner / Operator
- Firm Name
- LIFENET HEALTH
- Operator Number
- 9079121
- Address
- 1864 CONCERT DR., --
- City
- VIRGINIA BEACH
- State
- VA
- Postal Code
- 23453
- Country
- US
- Correspondent
- MICHAEL A PLEW
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) | MBP | Class 2 | Orthopedic | No | 2005-12-29 |
| Filler, Bone Void, Calcium Compound | MQV | Class 2 | Orthopedic | No | 2005-12-29 |
| Motor, Surgical Instrument, Ac-Powered | GEY | Class 1 | General, Plastic Surgery | No | 2013-01-30 |
| Suture, Nonabsorbable, Synthetic, Polyethylene | GAT | Class 2 | General, Plastic Surgery | No | 2007-08-27 |
| Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene | DXZ | Class 2 | Cardiovascular | No | 2008-12-10 |
Proprietary Names
Optium DBM
Vesuvius DBM Putty
I/C Graft Chamber
FlexiGRAFT GraftLink
FlexiGRAFT Sutured Lateral Ankle Tendon Construct
FlexiGRAFT GraftLink TS
FlexiGRAFT Connect EXT
FlexiGRAFT Connect
FlexiGRAFT QuadLink
FlexiGRAFT DualLink
CardioGRAFT-MC Decellularized Pulmonary Artery Patch
Establishment Types
Manufacture Medical Device
Manufacture Medical Device for Another Party (Contract Manufacturer)